Canonical Allele Identifier: CA162101874

Gene: ABCB1

Linked Data

• dbSNP Id: rs891770724
• gnomAD v2: 7-87145713-G-A
• gnomAD v3: 7-87516397-G-A
• gnomAD v4: 7-87516397-G-A
• MyVariant Identifiers: chr7:g.87145713G>A (hg19) ; chr7:g.87145713_87145718delinsATTTTA (hg19) ; chr7:g.87516397G>A (hg38) ; chr7:g.87516397_87516402delinsATTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516397G>A , CM000669.2:g.87516397G>A	GRCh38
NC_000007.13:g.87145713G>A , CM000669.1:g.87145713G>A	GRCh37
NC_000007.12:g.86983649G>A	NCBI36
NG_011513.1:g.201852C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3084+112C>T	ENSP00000265724.3:n.3084+112C>T
ENST00000622132.5:c.3084+112C>T MANE Select	ENSP00000478255.1:n.3084+112C>T
ENST00000265724.7:c.3084+112C>T	ENSP00000265724.3:n.3084+112C>T
ENST00000475929.5:n.240+112C>T
ENST00000488737.6:n.726+112C>T
ENST00000496821.5:n.712+112C>T
ENST00000543898.5:c.2892+112C>T	ENSP00000444095.1:n.2892+112C>T
ENST00000622132.4:c.3084+112C>T	ENSP00000478255.1:n.3084+112C>T
NM_000927.4:c.3084+112C>T	NP_000918.2:n.3084+112C>T
NM_001348944.1:c.3084+112C>T	NP_001335873.1:n.3084+112C>T
NM_001348945.1:c.3294+112C>T	NP_001335874.1:n.3294+112C>T
NM_001348946.1:c.3084+112C>T	NP_001335875.1:n.3084+112C>T
NM_001348946.2:c.3084+112C>T MANE Select	NP_001335875.1:n.3084+112C>T
NM_000927.5:c.3084+112C>T	NP_000918.2:n.3084+112C>T
NM_001348944.2:c.3084+112C>T	NP_001335873.1:n.3084+112C>T
NM_001348945.2:c.3294+112C>T	NP_001335874.1:n.3294+112C>T